PE Signal Research Articles

Removal of cardiac beat artifact in oesophageal pressure measurement by frequency analysis

Oesophageal pressure (Pes) measurements are important in medical research and useful in clinical diagnosis. Measurements, however, are contaminated heavily by cardiac artifacts. The spectrum and waveform of the Pes signal is obtained from the oesophageal balloon. Adaptive finite impulse response (AFIR) filter and modified adaptive noise cancellation (MANC) methods are adopted to filter out cardiac beat interference. These results are compared. In the frequency domain, frequency variations and spectral overlap between the Pes components and cardiac beat signal components impact on the performance of the filter. From our experimental results on power strength, the fourth or higher harmonics did not have any significant effect on the filter performance. However, the second harmonics of these signals had a significant effect on the filtering result. Thus, in the design of AFIR filters, attention is needed to minimise these effects. In frequency analysis, these harmonics or overlapping frequencies do not affect MANC. MANC was the better method for eliminating cardiac beat artifact in Pes measurement. The dynamic compliance (Cdyn) was also used to evaluate the performance of MANC and AFIR. The standard deviation of Cdyn was less than 0.15 using MANC, compared with standard deviations as high as 0.57 for AFIR. We conclude that MANC performs better than AFIR.

Photon echo experiments on 3–3′ diethylthiacarbocyanine in glass-forming liquids with ultrafast laser pulses

Photon echo experiments on diethylthiacarbocyanine iodide (DTCI) in dibuthylphthalate (DBP) and glycerol in the glass phase with femtosecond pulses are presented. The PE signal shows nonexponential decays even at low temperatures. This behavior is attributed to the many vibronic resonances of the chromophore/ glass system which can be simultaneously excited by the spectral bandwith of the laser pulses. We are able to extract from the PE decays the contribution of the homogeneous dephasing rate of the 0-0 transition of DTCI up to 20 K in dibutylphthalate and 40 K in glycerol. A beating structure in the echo decay for the system DTCI/DBP is also observed from 8 K up to 180 K (glass transition temperature for DBP). This feature is attributed to an intereference process involving excitation of a vibronic transition of DTCI characterized by a vibrational frequency of 300 cm-1.

Reduction of interlaboratory variability in flow cytometric immunophenotyping by standardization of instrument set-up and calibration, and standard list mode data analysis

Two workshops addressed the question to which degree standardization of instrument set-up and calibration, and standard list mode data analysis would reduce interlaboratory variability of flow cytometric results on prestained peripheral blood mononuclear cells (PBMC). Standard instrument set-up included uniform positioning of the "windows of analysis" for the forward and sideward light scatter and fluorescence (FL) 1 (i.e., fluorescein isothiocyanate [FITC]) and 2 (i.e., phycoerythrin [PE]) parameters. Reference standards and PBMC, double-stained with FITC- and PE-conjugated monoclonal antibodies covering a wide range of FL intensities and coexpression patterns, were sent out to 25 laboratories in Workshop 1 and to 35 laboratories in Workshop 2 with the following requests: a) to set up instruments according to local and standard protocols, b) to acquire list mode data on the PBMC with both instrument settings, and c) to analyze both datasets according to local protocols. Standard analysis of the list mode data acquired with uniform instrument settings was performed centrally using so-called "latent class model" software (Van Putten et al., Cytometry 14:86-96, 1993). This software provides an automated, "no-gating" analytical method of lymphocyte immunophenotypes and employs fixed FL marker settings as defined prior to each analytical run. In Workshop 1, these markers were set in identical histogram channels for all instruments based on results obtained with a reference instrument. Standard analysis of list mode data acquired after uniform instrument set-up led only to a 13% reduction of interlaboratory variability of results as compared to data analysis using local protocols. The standard protocol for instrument set-up led to uniform positioning of relatively strong FL signals but variable positioning of unstained cells on the FL histogram scales. Hence, standard FL marker settings were inappropriate for some instruments. Therefore, instrument responses to FITC and PE signals in Workshop 2 were calibrated using microbeads labeled with FITC or PE in a range of predefined FL intensities expressed in MESF units (molecules of equivalent soluble fluorochrome). That approach allowed the positioning of the FL markers for the standard analysis on the basis of identical FL1 and FL2 intensities, expressed in MESF units, for all instruments. Standard analysis of list mode data acquired after uniform instrument set-up and calibrated FL marker settings led to a 43% reduction of interlaboratory variability as compared to data analysis to local protocols. We conclude that standard list mode data analysis using fixed FL marker settings reduces the interlaboratory variability of flow cytometric results on prestained PBMC, provided that the instruments have been set up in a uniform way and that FL markers have been standardized on the basis of calibration of each instrument's response to the corresponding FL signals.

Reduction of interlaboratory variability in flow cytometric immunophenotyping by standardization of instrument set‐up and calibration, and standard list mode data analysis

Two workshops addressed the question to which degree standardization of instrument set-up and calibration, and standard list mode data analysis would reduce interlaboratory variability of flow cytometric results on prestained peripheral blood mononuclear cells (PBMC). Standard instrument set-up included uniform positioning of the “windows of analysis” for the forward and sideward light scatter and fluorescence (FL) 1 (i.e., fluorescein isothiocyanate [FITC]) and 2 (i.e., phycoerythrin [PE]) parameters. Reference standards and PBMC, double-stained with FITC- and PE-conjugated monoclonal antibodies covering a wide range of FL intensities and coexpression patterns, were sent out to 25 laboratories in Workshop 1 and to 35 laboratories in Workshop 2 with the following requests: a) to set up instruments according to local and standard protocols, b) to acquire list mode data on the PBMC with both instrument settings, and c) to analyze both datasets according to local protocols. Standard analysis of the list mode data acquired with uniform instrument settings was performed centrally using so-called “latent class model” software (Van Putten et al., Cytometry 14:86–96, 1993). This software provides an automated, “no-gating” analytical method of lymphocyte immunophenotypes and employs fixed FL marker settings as defined prior to each analytical run. In Workshop 1, these markers were set in identical histogram channels for all instruments based on results obtained with a reference instrument. Standard analysis of list mode data acquired after uniform instrument set-up led only to a 13% reduction of interlaboratory variability of results as compared to data analysis using local protocols. The standard protocol for instrument set-up led to uniform positioning of relatively strong FL signals but variable positioning of unstained cells on the FL histogram scales. Hence, standard FL marker settings were inappropriate for some instruments. Therefore, instrument responses to FITC and PE signals in Workshop 2 were calibrated using microbeads labeled with FITC or PE in a range of predefined FL intensities expressed in MESF units (molecules of equivalent soluble fluorochrome). That approach allowed the positioning of the FL markers for the standard analysis on the basis of identical FL1 and FL2 intensities, expressed in MESF units, for all instruments. Standard analysis of list mode data acquired after uniform instrument set-up and calibrated FL marker settings led to a 43% reduction of interlaboratory variability as compared to data analysis to local protocols. We conclude that standard list mode data analysis using fixed FL marker settings reduces the interlaboratory variability of flow cytometric results on prestained PBMC, provided that the instruments have been set up in a uniform way and that FL markers have been standardized on the basis of calibration of each instrument's response to the corresponding FL signals. Cytometry 30:10–22, 1997. © 1997 Wiley-Liss, Inc.

Avrami's kinetic approach for describing Volmer Weber growth mode at solid surfaces studied via PES and AES

A model is presented for describing the time dependence of the photoelectron and/or Auger signals during the overlayer formation in the case of Volmer Weber growth mode, i.e. 3D island formation. The impingement among clusters has been taken into account in the framework of Avrami's statistical approach. A first system has been considered in which nucleation occurs at a given number of preexisting sites randomly distributed throughout the whole surface. The results obtained by numerical computations indicate that particular conditions can be indeed realized for which the PES signal is chiefly related to the kinetics of the surface fraction that is covered by islands. A more involved system has been also modeled where nucleation does not occur at preexisting sites but through the formation of stable dimers. Under this circumstance, Avrami's treatment of island impingement can be still retained although now a system of integral differential equations has to be solved to get the kinetics. Such a modelling should be suitable for describing the metallic film growth studied by PES.

Photoelectron spectroscopy of f-element organometallic complexes. 6. Electronic structure of tetrakis(cyclopentadienyl)actinide complexes

A description of the electronic structure of M(eta/sup 5/-C/sub 5/H/sub 4/CH/sub 3/)/sub 4/ (M = Th, U) complexes as based upon He I and He II photoelectron spectra and relativistic X..cap alpha..-SW calculations is presented. Despite the true S/sub 4/ symmetry of the molecules, the outermost MO's are grouped as if the complexes have a pure tetrahedral ligation environment. As a consequence, donation to empty metal orbitals appears to be highly dominated by the symmetry requirements. The HOMO in Cp'/sub 4/U is almost pure 5f in character, and the corresponding /sup 2/F/sub 5/2/ final state produced upon ionization is split by operation of a T/sub d/ ligand field. The relative intensity variations observed on passing from He I to He II spectra are quite unexpected. It appears that the He II increases of PE signals due to MO's having large metal 6d character are greater than those due to MO's having comparable 5f admixture.